34 results on '"O'Donovan, Michael"'
Search Results
2. The Duffy-null genotype and risk of infection
3. A transcriptome-wide association study implicates specific pre- and post-synaptic abnormalities in schizophrenia
4. Support for the involvement of large copy number variants in the pathogenesis of schizophrenia
5. A network of dopaminergic gene variations implicated as risk factors for schizophrenia
6. Evidence that common variation in NEDD9 is associated with susceptibility to late-onset Alzheimerʼs and Parkinsonʼs disease
7. A transcriptome-wide association study implicates specific pre- and post-synaptic abnormalities in schizophrenia.
8. Comprehensive analysis of schizophrenia-associated loci highlights ion channel pathways and biologically plausible candidate causal genes
9. De novo CNVs in bipolar affective disorder and schizophrenia
10. Amyotrophic lateral sclerosis-related VAPB P56S mutation differentially affects the function and survival of corticospinal and spinal motor neurons
11. A genome-wide study shows a limited contribution of rare copy number variants to Alzheimer's disease risk
12. Common variants at VRK2 and TCF4 conferring risk of schizophrenia
13. A large replication study and meta-analysis in European samples provides further support for association of AHI1 markers with schizophrenia
14. Cis- and trans- loci influence expression of the schizophrenia susceptibility gene DTNBP1
15. Evidence that common variation in NEDD9 is associated with susceptibility to late-onset Alzheimer's and Parkinson's disease
16. A network of dopaminergic gene variations implicated as risk factors for schizophrenia
17. Strong evidence that GNB1L is associated with schizophrenia
18. Genome-wide linkage analysis of 723 affected relative pairs with late-onset Alzheimer's disease
19. Evidence for novel susceptibility genes for late-onset Alzheimer's disease from a genome-wide association study of putative functional variants
20. DAPK1 variants are associated with Alzheimer's disease and allele-specific expression
21. The genetics of attention deficit hyperactivity disorder
22. Haplotypes at the dystrobrevin binding protein 1 (DTNBP1) gene locus mediate risk for schizophrenia through reduced DTNBP1 expression
23. Allelic expression of APOE in human brain: effects of epsilon status and promoter haplotypes
24. A genome-wide study shows a limited contribution of rare copy number variants to Alzheimer's disease risk.
25. Most genome-wide significant susceptibility loci for schizophrenia and bipolar disorder reported to date cross-traditional diagnostic boundaries.
26. Strong evidence that GNB1L is associated with schizophrenia.
27. Comparative genome hybridization suggests a role for NRXN1 and APBA2 in schizophrenia.
28. Functional analysis of human promoter polymorphisms.
29. Recent advances in the genetics of schizophrenia.
30. Experimental analysis of the annotation of promoters in the public database.
31. ATP2A2 mutations in Darier's disease and their relationship to neuropsychiatric phenotypes.
32. Amyotrophic lateral sclerosis-related VAPB P56S mutation differentially affects the function and survival of corticospinal and spinal motor neurons.
33. An inherited duplication at the gene p21 Protein-Activated Kinase 7 (PAK7) is a risk factor for psychosis.
34. CNV analysis in a large schizophrenia sample implicates deletions at 16p12.1 and SLC1A1 and duplications at 1p36.33 and CGNL1.
Catalog
Books, media, physical & digital resources
Discovery Service for Jio Institute Digital Library
For full access to our library's resources, please sign in.